MSX2 and RUNX2

  • Number of citations of the paper that reports this interaction (PMID 11683913)
  • 20
  • Data Source:
  • BioGRID (affinity chromatography technology)
  • HPRD (in vitro, in vivo)

MSX2

RUNX2

Gene Name msh homeobox 2 runt-related transcription factor 2
Image No pdb structure No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 21 interactors: ATXN1 CEBPA DLX2 DLX5 GTF2F1 GTF2F2 MAGED1 MSX1 NR3C1 PIAS2 POLR3D POU2AF1 PPARG RUNX2 SPEN TLE1 TLE2 XRCC5 XRCC6 ZBTB17 ZDHHC2 36 interactors: ALYREF AR AXIN1 CBFB CCNB1 CDK1 CEBPB DVL2 EP300 ETS1 FHL2 FOS HDAC3 HDAC4 HDAC6 HIF1A HIVEP3 JUN KAT6B LEF1 MAP3K4 MSX2 PRKCD RB1 RBM14 SMAD2 SMAD3 SMAD6 SMURF2 SOX9 STUB1 TAF1A UBTF XRCC5 XRCC6 YAP1
Entrez ID 4488 860
HPRD ID 00421 02566
Ensembl ID ENSG00000120149 ENSG00000124813
Uniprot IDs P35548 F8W8U5 Q13950 Q32MY8
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?
achondroplasia  attendant  clefts  collins  craniosynostosis  crest  crouzon  deformities  dentofacial  detoxifying  excessively  ganglionic  hemifacial  holoprosencephaly  jaws  kills  malocclusions  merging  microsomia  mismatches  neuromeres  ordinated  palatal  placodal  placodes  prominences  radically  shelves  treacher 
1q22  aml  correlative  cytogenetic  decitabine  demethylating  elucidate  epigenetics  frequent  haematological  hypermethylation  inactivation  inv  leukaemia  leukaemias  lymphocytic  malignancies  methylated  mostly  myelodysplatic  p13  promoters  re  relapse  runx1  runx3  syndromes  unmethylated 
Tagcloud (Difference) ?
achondroplasia  attendant  clefts  collins  craniosynostosis  crest  crouzon  deformities  dentofacial  detoxifying  excessively  ganglionic  hemifacial  holoprosencephaly  jaws  kills  malocclusions  merging  microsomia  mismatches  neuromeres  ordinated  palatal  placodal  placodes  prominences  radically  shelves  treacher 
1q22  aml  correlative  cytogenetic  decitabine  demethylating  elucidate  epigenetics  frequent  haematological  hypermethylation  inactivation  inv  leukaemia  leukaemias  lymphocytic  malignancies  methylated  mostly  myelodysplatic  p13  promoters  re  relapse  runx1  runx3  syndromes  unmethylated 
Tagcloud (Intersection) ?